Midodrine Hydrochloride
- Product NDC
- 72162-1517
- 11-digit product format
- 721621517
- Labeler code
- 72162
- Product ID
- 72162-1517_c4296ad6-f454-4e6e-bf0b-2c1fc5d7271e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Midodrine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA207169
- Marketing category
- ANDA
- Marketing start
- 2018-10-29
- Substance
- MIDODRINE HYDROCHLORIDE
- Active strength
- 2.5 mg/1
- Pharmacologic classes
- Adrenergic alpha-Agonists [MoA], alpha-Adrenergic Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 59JV96YTXV | MIDODRINE HYDROCHLORIDE | 43218-56-0 | MIDODRINE HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-1517-1 | 72162151701 | 100 TABLET in 1 BOTTLE (72162-1517-1) | 100 tablet | 2023-10-06 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Midodrine Hydrochloride | Bryant Ranch Prepack | 2023-10-06 | HUMAN PRESCRIPTION DRUG LABEL | 100 |